JPH0684622A - Radio wave absorber - Google Patents

Radio wave absorber

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Publication number
JPH0684622A
JPH0684622A JP4236925A JP23692592A JPH0684622A JP H0684622 A JPH0684622 A JP H0684622A JP 4236925 A JP4236925 A JP 4236925A JP 23692592 A JP23692592 A JP 23692592A JP H0684622 A JPH0684622 A JP H0684622A
Authority
JP
Japan
Prior art keywords
radio wave
oxide
reflection coefficient
monoxide
less
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP4236925A
Other languages
Japanese (ja)
Inventor
Masao Shigihara
政夫 鴫原
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tokin Corp
Original Assignee
Tokin Corp
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Filing date
Publication date
Application filed by Tokin Corp filed Critical Tokin Corp
Priority to JP4236925A priority Critical patent/JPH0684622A/en
Publication of JPH0684622A publication Critical patent/JPH0684622A/en
Withdrawn legal-status Critical Current

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  • Soft Magnetic Materials (AREA)
  • Shielding Devices Or Components To Electric Or Magnetic Fields (AREA)

Abstract

PURPOSE:To realize a magnetic material excellent in radio wave absorbing characteristics in which reflection coefficient can be kept high over a wide frequency region by adding specified quantities of titanium dioxide, vanadium pentaoxide, and hafnium oxide. CONSTITUTION:Zinc oxide ZnO, nickel monoxide NiO, and copper monoxide CuO are contained as main constituents while ferric oxide Fe2O3 is contained as the remainder and one or both of silicon dioxide SiO2 and manganese monoxide MnO is further contained as subconstituent. Furthermore titanium dioxide TiO2, vanadium pentaoxide V2O5 and hafnium oxide are contained, respectively, upto 0.30wt.%, 0.20wt.% and 1.00wt.% as additives. This composition provides an oxide magnetic material for absorbing radio wave having significantly improved radio wave absorbing characteristics in which the region where the value of radio wave reflection coefficient is lower than -20dB is widened in the frequency region higher than 400MHz and low dielectric constant is achieved.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は電波暗室に使用される3
0〜1000MHzの周波数領域で用いる、主としてフ
ェライト電波吸収体の材料であるNi−Cu−Zn系酸
化物磁性材料に関し、特に主成分として32.0〜3
5.0mol%の酸化亜鉛(以下ZnOと称す)、1
0.0〜12.0mol%の一酸化ニッケル(Ni
O)、5.0〜7.0mol%の一酸化銅(CuO)、
及び残部酸化第2鉄(Fe2 3 )を含み、副成分とし
て0.05wt%以下の二酸化珪素(SiO2 )と0.
10wt%以下の一酸化マンガン(MnO)の夫々1種
又は2種の成分を含む電波吸収体用酸化物磁性材料の改
良に関するものである。
This invention is used in an anechoic chamber.
A Ni-Cu-Zn-based oxide magnetic material used as a material for a ferrite electromagnetic wave absorber, which is used in a frequency range of 0 to 1000 MHz, and particularly 32.0 to 3 as a main component.
5.0 mol% zinc oxide (hereinafter referred to as ZnO), 1
0.0-12.0 mol% nickel monoxide (Ni
O), 5.0 to 7.0 mol% of copper monoxide (CuO),
And the balance ferric oxide (Fe 2 O 3 ), and 0.05 wt% or less of silicon dioxide (SiO 2 ) as a subcomponent and 0.
The present invention relates to an improvement of an oxide magnetic material for radio wave absorbers containing one or two components of manganese monoxide (MnO) of 10 wt% or less.

【0002】[0002]

【従来の技術】従来この種のフェライト電波吸収体を製
造する場合には、主成分である酸化亜鉛(ZnO)、一
酸化ニッケル(NiO)、一酸化銅(CuO)、及び酸
化第二鉄(Fe2 3 )の粉末と、副成分である0.0
5wt%以下の二酸化珪素(SiO2 )、0.10wt
%以下の一酸化マンガン(MnO)の1種又は2種の粉
末とを混合、成形後、大気中の雰囲気で1050℃〜1
170℃の温度範囲で2時間程度保持し焼結を行うこと
により、Ni−Cu−Zn系酸化物磁性材料の焼結体と
していた。
2. Description of the Related Art Conventionally, in the case of manufacturing this kind of ferrite electromagnetic wave absorber, zinc oxide (ZnO), nickel monoxide (NiO), copper monoxide (CuO), and ferric oxide ( Fe 2 O 3 ) powder and an auxiliary component of 0.0
5 wt% or less of silicon dioxide (SiO 2 ), 0.10 wt
% Or less of one or two kinds of manganese monoxide (MnO) powder, and after molding and molding, 1050 ° C. to 1 in an air atmosphere.
A Ni—Cu—Zn-based oxide magnetic material sintered body was obtained by holding the material in the temperature range of 170 ° C. for about 2 hours and performing sintering.

【0003】[0003]

【発明が解決しようとする課題】上記のようにして得ら
れた焼結体を電波暗室の内壁に貼ると、整合厚にした時
でも反射係数が−20dB以下の周波数領域は50〜4
00MHzである。そこで400MHz以上の周波数領
域はウレタン吸収体を使用していた。しかしながら、整
合するまでウレタン吸収体を増していくと、その長さが
大となって使用困難になってくる欠点があった。
When the sintered body obtained as described above is attached to the inner wall of the anechoic chamber, the frequency range where the reflection coefficient is -20 dB or less is 50 to 4 even when the thickness is adjusted.
It is 00 MHz. Therefore, the urethane absorber is used in the frequency region of 400 MHz or higher. However, if the number of urethane absorbers is increased until they are aligned, the length thereof becomes large, which makes it difficult to use.

【0004】したがって本発明は酸化物磁性体の焼結体
のみで500MHz程度或いはそれ以上の広い周波数領
域で反射係数を−20dB以下に保つことの可能な、電
波吸収特性の良い磁性材料を提供しようとするものであ
る。
Therefore, the present invention is to provide a magnetic material having a good electromagnetic wave absorption property, which can maintain the reflection coefficient of -20 dB or less in a wide frequency range of about 500 MHz or more with only a sintered body of an oxide magnetic material. It is what

【0005】[0005]

【課題を解決するための手段】本発明の電波吸収体は、
主成分として32.0〜35.0mol%の酸化亜鉛
(ZnO)、10.0〜12.0mol%の一酸化ニッ
ケル(NiO)、5.0〜7.0mol%の一酸化銅
(CuO)、及び残部酸化第2鉄(Fe2 3 )を含
み、副成分として0.05wt%以下(0.0wt%を
含まず)の二酸化珪素(SiO2 )、0.10wt%以
下(0.0wt%を含まず)の一酸化マンガン(Mn
O)の夫々1種又は2種の成分を含む電波吸収体用酸化
物磁性材料において、0.30wt%以下(0.0%を
含まず)の二酸化チタン(TiO2 )、0.20wt%
以下(0.0wt%を含まず)の五酸化バナジウム(V
2 5 )及び1.00wt%以下(0.0wt%を含ま
ず)の酸化ハフニウム(HfO2 )を添加物として含む
ことを特徴とする。
The radio wave absorber of the present invention comprises:
32.0 to 35.0 mol% zinc oxide (ZnO) as a main component, 10.0 to 12.0 mol% nickel monoxide (NiO), 5.0 to 7.0 mol% copper monoxide (CuO), And the balance of ferric oxide (Fe 2 O 3 ), and 0.05 wt% or less (not including 0.0 wt%) of silicon dioxide (SiO 2 ) as a sub-component, 0.10 wt% or less (0.0 wt%) Manganese monoxide (Mn not included)
O) in the oxide magnetic material for a radio wave absorber containing one or two components respectively, titanium dioxide (TiO 2 ) of 0.30 wt% or less (not including 0.0%), 0.20 wt%
The following (not including 0.0 wt%) vanadium pentoxide (V
2 O 5 ) and hafnium oxide (HfO 2 ) of 1.00 wt% or less (not including 0.0 wt%) as additives.

【0006】[0006]

【作用】添加物V2 5 及びHfO2 は、大気中の雰囲
気で1050℃〜1170℃の温度範囲で2時間保持
し、焼結を行うことにより、それそれぞれ粒界に析出
し、粒界の抵抗率を増加させ、又添加物TiO2 は、前
記の焼結処理により、結晶内に固溶し、結晶内部の抵抗
率を増加させ、さらに結晶組織を均一にする使用がある
と考えられる。これら3つの添加物を含むNi−Cu−
Zn系酸化物磁性材料は、先に説明した副成分の効果に
加えて、組織内部の電磁気特性が均一化され、反射係数
が−20dB以下の周波数領域が広く、低い誘電率の値
を示すものと考えられる。
The additives V 2 O 5 and HfO 2 are precipitated in the grain boundaries respectively by holding the additives V 2 O 5 and HfO 2 in the atmosphere in the temperature range of 1050 ° C. to 1170 ° C. for 2 hours and sintering. It is thought that the additive TiO 2 is used as a solid solution in the crystal by the above-mentioned sintering treatment to increase the resistivity inside the crystal and further to make the crystal structure uniform. . Ni-Cu- containing these three additives
In addition to the effect of the sub-components described above, the Zn-based oxide magnetic material has a uniform electromagnetic property inside the tissue, has a wide frequency range with a reflection coefficient of -20 dB or less, and exhibits a low dielectric constant value. it is conceivable that.

【0007】[0007]

【実施例】以下に本発明の実施例及び比較例について実
験内容を詳しく説明する。酸化物粉末を混合、成形、焼
成してなる酸化物磁性材料の標準主成分として、50.
0mol%の酸化第二鉄(Fe2 3 )、32.0mo
l%の酸化亜鉛(ZnO)、12.0mol%の酸化ニ
ッケル(NiO)、及び6.0mol%の一酸化銅(C
uO)を含有し、副成分として、0.05wt%以下の
二酸化ケイ素(SiO2 )及び0.10wt%以下の一
酸化マンガン(MnO)を含有する従来からあるNi−
Cu−Zn系酸化物磁性材料に、二酸化チタン(TiO
2 )、五酸化バナジウム(V2 5 )、及び酸化ハフニ
ウム(HfO2 )の添加物を種々の割合で複合添加した
複数の第1の実施例のNi−Cu−Zn系酸化物磁性材
料を各種試作し、この標準比較例として、上記添加物を
添加しない従来のNi−Cu−Zn系酸化物磁性材料、
及び第1の比較例として上記添加物を単独又は複合添加
した複数のNi−Cu−Zn系酸化物磁性材料を試作し
た。
[Examples] The details of the experiments of Examples and Comparative Examples of the present invention will be described below. As a standard main component of an oxide magnetic material obtained by mixing, molding and firing oxide powder, 50.
0 mol% of ferric oxide (Fe 2 O 3), 32.0mo
1% zinc oxide (ZnO), 12.0 mol% nickel oxide (NiO), and 6.0 mol% copper monoxide (C).
uO) and, as secondary components, 0.05% by weight or less of silicon dioxide (SiO 2 ) and 0.10% by weight or less of manganese monoxide (MnO).
Cu-Zn oxide magnetic material, titanium dioxide (TiO 2
2 ), vanadium pentoxide (V 2 O 5 ), and hafnium oxide (HfO 2 ) are added in various proportions in a combined manner to form a plurality of Ni-Cu-Zn-based oxide magnetic materials of the first embodiment. Various prototypes were manufactured, and as a standard comparative example, a conventional Ni-Cu-Zn-based oxide magnetic material without the addition of the above additives,
As a first comparative example, a plurality of Ni—Cu—Zn-based oxide magnetic materials to which the above additives were added alone or in combination were manufactured.

【0008】これらの実施例及び比較例の試作に於て
は、それぞれの酸化物原料を所定量秤量し、混合、予備
焼成、造粒し、成形プレス後、大気中において、110
0℃で2時間焼成した。各周波数の電波における反射係
数は各組成の異なる材料毎に、外径19.8mm、内径
8.6mm、同軸管法により測定した。
In the trial production of these examples and comparative examples, a predetermined amount of each oxide raw material was weighed, mixed, pre-baked, granulated, and after molding and pressing, 110 in the atmosphere.
It was calcined at 0 ° C. for 2 hours. The reflection coefficient of radio waves of each frequency was measured by the coaxial tube method for each material having a different composition with an outer diameter of 19.8 mm, an inner diameter of 8.6 mm.

【0009】下記の表1は試作した第1の実施例の試料
No.8〜10,No.12,13,15,16と、標
準比較例として試料No.1と、第1の比較例として試
料No.2〜7,No.11,14,17とについて、
それぞれの副成分及び添加物の含有量と反射係数が−2
0dB以下の周波数領域の範囲を示したものである。
Table 1 below shows the sample No. of the first embodiment that was prototyped. 8-10, No. 12, 13, 15, 16 and sample No. 1 as a standard comparative example. 1 and sample No. 1 as a first comparative example. 2-7, No. About 11, 14, 17 and
The content and reflection coefficient of each subcomponent and additive is -2.
It shows the range of the frequency region of 0 dB or less.

【0010】[0010]

【表1】 [Table 1]

【0011】表1によれば、添加物である二酸化チタン
(TiO2 )、五酸化バナジウム(V2 5 )及び酸化
ハフニウム(HfO2 )の複合添加により、誘電率は従
来の標準比較例の試料No.1より低く、反射係数(−
20dB以下)の周波数領域の範囲はより広いことがわ
かる。これは上記の3つの添加物のうち、TiO2 とH
fO2 はNi−Cu−Zn系酸化物磁性材料の粒界に析
出して粒界の抵抗率を増大させ、V2 5 は結晶内に固
溶して結晶内の抵抗率の増大及び結晶組織の均一化に効
果があるものと考えられ、これらの複合作用によって組
織内部の電磁気特性を均一化し、組織全体の抵抗率を増
大し、反射係数(−20dB以下)の周波数領域を広く
したものと考えられる。
According to Table 1, the dielectric constant of the conventional standard comparative example is increased by the combined addition of titanium dioxide (TiO 2 ), vanadium pentoxide (V 2 O 5 ) and hafnium oxide (HfO 2 ) which are additives. Sample No. Lower than 1, the reflection coefficient (-
It can be seen that the range of the frequency region of 20 dB or less) is wider. Of the above three additives, TiO 2 and H
fO 2 precipitates at the grain boundaries of the Ni—Cu—Zn-based oxide magnetic material to increase the resistivity of the grain boundaries, and V 2 O 5 forms a solid solution in the crystals to increase the resistivity in the crystals and the crystals. It is considered to be effective for tissue homogenization, and the electromagnetic effect inside the tissue is homogenized by these combined actions, the resistivity of the whole tissue is increased, and the frequency range of the reflection coefficient (-20 dB or less) is widened. it is conceivable that.

【0012】又表1に於て、TiO2 を0.40wt%
添加した試料No.11、V2 5を0.30wt%添
加した試料No.14、及びHfO2 を1.10wt%
添加した試料No.17に於ては、異常粒の成長が認め
られ、そのため電力損失や誘電率が大きくなったと考え
られる。さらに、表1の試料No.2〜7は、それぞれ
添加物の単独又は2つが0.0%であり、この場合も電
力損失や誘電率が大きく、効果が薄いことが判る。
In Table 1, 0.40 wt% of TiO 2 is added.
Added sample No. 11, sample No. 11 to which 0.30 wt% of V 2 O 5 was added. 14, and 1.10 wt% of HfO 2.
Added sample No. In No. 17, it is considered that abnormal grain growth was observed, which resulted in increased power loss and dielectric constant. Further, the sample No. It is understood that 2 to 7 each have 0.0% of the additive alone or two of them, and in this case as well, the power loss and the dielectric constant are large and the effect is small.

【0013】下記の表2は、従来の標準比較例の試料N
o.1と本発明の実施例の試料No.8〜17につい
て、それぞれの各添加物の添加量に対する各周波数に於
ける反射係数との関係を示す。
Table 2 below shows sample N of the conventional standard comparative example.
o. 1 and the sample No. 1 of the embodiment of the present invention. 8 to 17, the relationship between the amount of each additive added and the reflection coefficient at each frequency is shown.

【0014】[0014]

【表2】 [Table 2]

【0015】表2によると、二酸化チタン(TiO2
の添加量を増加するに従って、低い周波数域においては
電波の反射係数の値が大きくなり電波の吸収特性が向上
するが、高い周波数域においては逆に劣化する傾向が見
られる。二酸化チタン(TiO)0.30wt%添加し
た時に於いては、500MHzに於いて反射係数が−2
0dBの値が得られ、しかも50MHzに於ける反射係
数が−30.1dBという、従来の無添加品より優れた
電波吸収体用酸化物磁性材料が得られた。
According to Table 2, titanium dioxide (TiO 2 )
As the addition amount of is increased, the value of the reflection coefficient of the radio wave is increased in the low frequency range and the absorption characteristics of the radio wave is improved, but it tends to be deteriorated in the high frequency range. When 0.30 wt% of titanium dioxide (TiO) is added, the reflection coefficient is -2 at 500 MHz.
A value of 0 dB was obtained, and a reflection coefficient at 50 MHz was -30.1 dB, which was superior to the conventional additive-free product, and an oxide magnetic material for a radio wave absorber was obtained.

【0016】五酸化バナジウム(V2 5 )及び酸化ハ
フニウム(HfO2 )の添加量を増加するに従って、高
い周波数域においては電波の反射係数の値が大きくなっ
て電波の吸収特性に優れた材料が得られるが、低い周波
数域においては電波の反射係数の値が大きくなって劣化
の傾向が見られる。五酸化バナジウム(V2 5 )0.
20wt%添加した時及び酸化ハフニウム(HfO2
1.00wt%添加した時、従来の無添加品より優れた
電波吸収体用酸化物磁性材料が得られた。
As the added amount of vanadium pentoxide (V 2 O 5 ) and hafnium oxide (HfO 2 ) is increased, the value of the reflection coefficient of the radio wave is increased in a high frequency range, and the material has excellent radio wave absorption characteristics. However, in the low frequency range, the value of the reflection coefficient of the radio wave becomes large and the deterioration tendency is seen. Vanadium pentoxide (V 2 O 5 ) 0.
When 20 wt% is added and hafnium oxide (HfO 2 )
When 1.00 wt% was added, an oxide magnetic material for a wave absorber superior to the conventional non-added product was obtained.

【0017】電波の吸収特性を示す反射係数の値は、二
酸化チタン(TiO)の添加量を増すと50MHz付近
に於いて大きくなり、反射係数が最大となる周波数は低
い周波数へと移って行く結果を示している。これらの特
性値で反射係数が最大となる周波数の移動は表1に示す
誘電率の値に符合しており、誘電率が最小値を示す二酸
化チタン(TiO2 )添加組成に於て、最大の反射係数
の値と最大の反射係数を示す周波数として最も高い周波
数を示している。
The value of the reflection coefficient showing the electromagnetic wave absorption characteristics becomes large at around 50 MHz as the amount of titanium dioxide (TiO) added increases, and the frequency at which the reflection coefficient becomes maximum shifts to a lower frequency. Is shown. The shift of the frequency at which the reflection coefficient is maximum at these characteristic values corresponds to the value of the dielectric constant shown in Table 1, and is the maximum at the titanium dioxide (TiO 2 ) additive composition having the minimum dielectric constant. The highest frequency is shown as the value showing the value of the reflection coefficient and the maximum reflection coefficient.

【0018】又、五酸化バナジウム(V2 5 )、酸化
ハフニウム(HfO2 )の添加量を増すと500MHz
付近に於ける反射係数の値は大きくなり、反射係数が最
大となる周波数は高い周波数へと移って行く結果を示し
ている。これらの特性値で反射係数が最大となる周波数
の移動は表1に示す誘電率の値に符合しており、誘電率
が最小値を示す五酸化バナジウム(V2 5 )及び酸化
ハフニウム(HfO2)の添加組成に於て、最大の反射
係数の値と反射係数を示す周波数として最も高い周波数
を示している。
Further, if the addition amounts of vanadium pentoxide (V 2 O 5 ) and hafnium oxide (HfO 2 ) are increased, it becomes 500 MHz.
The value of the reflection coefficient in the vicinity increases, and the frequency at which the reflection coefficient becomes maximum shows a result of shifting to a higher frequency. The shift of the frequency at which the reflection coefficient becomes maximum at these characteristic values matches the value of the dielectric constant shown in Table 1, and vanadium pentoxide (V 2 O 5 ) and hafnium oxide (HfO) at which the dielectric constant shows the minimum value. In the additive composition of 2 ), the highest reflection coefficient and the highest frequency are shown.

【0019】[0019]

【発明の効果】本発明によれば、従来のニッケル、銅、
亜鉛、鉄系酸化物材料に0.30wt%以下(0.0w
t%を含まず)の二酸化チタン(TiO2 )、0.20
wt%以下(0.0wt%を含まず)の五酸化バナジウ
ム(V2 5 )、及び1.00wt%以下(0.0wt
%を含まず)の酸化ハフニウム(HfO2 )を添加する
ことにより、従来のニッケル、銅、亜鉛、鉄系酸化物磁
性材料に比べて、電波の反射係数の値が特に400MH
z以上の周波数領域に於て−20dB以下の領域が広が
り、電波吸収特性を大幅に改良した電波吸収体用酸化物
磁性材料が得られた。
According to the present invention, conventional nickel, copper,
0.30wt% or less (0.0w
titanium dioxide containing not) a t% (TiO 2), 0.20
Vanadium pentoxide (V 2 O 5 ) of wt% or less (not including 0.0 wt%), and 1.00 wt% or less (0.0 wt%)
% Of hafnium oxide (HfO 2 ) is added, the value of the reflection coefficient of the radio wave is 400 MH compared with the conventional nickel, copper, zinc, and iron oxide magnetic materials.
In the frequency range of z or more, the range of -20 dB or less was widened, and an oxide magnetic material for a radio wave absorber having a significantly improved radio wave absorption characteristic was obtained.

【0020】従って本発明による電波吸収体用酸化物磁
性材料を用いた場合にはより広い帯域の電波吸収体に適
用でき、小型で低価格な電波暗室を構成出来る。
Therefore, when the oxide magnetic material for a radio wave absorber according to the present invention is used, it can be applied to a radio wave absorber having a wider band, and a small anechoic chamber can be constructed at a low price.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明による電波吸収体の、二酸化チタン(T
iO2 )の、添加量が0.0wt%(比較例)、0.1
0wt%、0.30wt%、及び0.40wt%の場合
の、30MHz〜600MHz範囲に於ける周波数と反
射係数の関係を示す特性図。
FIG. 1 shows a titanium dioxide (T) of a radio wave absorber according to the present invention.
iO 2 ) is added in an amount of 0.0 wt% (comparative example), 0.1
The characteristic view which shows the relationship between the frequency and the reflection coefficient in 30MHz-600MHz range in case of 0 wt%, 0.30 wt%, and 0.40 wt%.

【図2】本発明による電波吸収体の、五酸化バナジウム
(V2 5 )の添加量が0.0wt%(比較例)、0.
10wt%、0.20wt%、及び0.30wt%の場
合の、30MHz〜600MHz範囲に於ける周波数と
反射係数の関係を示す特性図。
FIG. 2 shows the radio wave absorber according to the present invention in which vanadium pentoxide (V 2 O 5 ) was added in an amount of 0.0 wt% (comparative example), 0.
The characteristic view which shows the relationship between the frequency and the reflection coefficient in 30MHz-600MHz range in case of 10 wt%, 0.20 wt%, and 0.30 wt%.

【図3】本発明による電波吸収体の、酸化ハフニウム
(HfO2 )の添加量が0.0wt%(比較例)、0.
80wt%、1.00wt%、及び1.10wt%の場
合の、30MHz〜600MHz範囲に於ける周波数と
反射係数の関係を示す特性図。
FIG. 3 is a radio wave absorber according to the present invention in which the amount of hafnium oxide (HfO 2 ) added is 0.0 wt% (comparative example);
The characteristic view which shows the relationship between the frequency and the reflection coefficient in 30MHz-600MHz range in case of 80 wt%, 1.00 wt%, and 1.10 wt%.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 主成分として32.0〜35.0mol
%の酸化亜鉛(ZnO)、10.0〜12.0mol%
の一酸化ニッケル(NiO)、5.0〜7.0mol%
の一酸化銅(CuO)、及び残部酸化第2鉄(Fe2
3 )を含み、副成分として0.05wt%以下(0.0
wt%を含まず)の二酸化珪素(SiO2 )、0.10
wt%以下(0.0wt%を含まず)の一酸化マンガン
(MnO)の夫々1種又は2種の成分を含む電波吸収体
用酸化物磁性材料において、 0.30wt%以下(0.0%を含まず)の二酸化チタ
ン(TiO2 )、0.20wt%以下(0.0wt%を
含まず)の五酸化バナジウム(V2 5 )及び1.00
wt%以下(0.0wt%を含まず)の酸化ハフニウム
(HfO2 )を添加物として含むことを特徴とする電波
吸収体。
1. A main component of 32.0 to 35.0 mol
% Zinc oxide (ZnO), 10.0-12.0 mol%
Nickel monoxide (NiO), 5.0-7.0 mol%
Copper monoxide (CuO), and the balance ferric oxide (Fe 2 O)
3 ) and contains 0.05 wt% or less (0.0
(not including wt%) silicon dioxide (SiO 2 ), 0.10
0.30 wt% or less (0.0%) in an oxide magnetic material for a radio wave absorber containing one or two components of manganese monoxide (MnO) of not more than wt% (not including 0.0 wt%), respectively. Titanium dioxide (TiO 2 ), vanadium pentoxide (V 2 O 5 ) 0.20 wt% or less (not including 0.0 wt%) and 1.00
A radio wave absorber comprising hafnium oxide (HfO 2 ) in an amount of wt% or less (not including 0.0 wt%) as an additive.
JP4236925A 1992-09-04 1992-09-04 Radio wave absorber Withdrawn JPH0684622A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4236925A JPH0684622A (en) 1992-09-04 1992-09-04 Radio wave absorber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4236925A JPH0684622A (en) 1992-09-04 1992-09-04 Radio wave absorber

Publications (1)

Publication Number Publication Date
JPH0684622A true JPH0684622A (en) 1994-03-25

Family

ID=17007788

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4236925A Withdrawn JPH0684622A (en) 1992-09-04 1992-09-04 Radio wave absorber

Country Status (1)

Country Link
JP (1) JPH0684622A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1006610A2 (en) * 1998-12-04 2000-06-07 TDK Corporation Radio wave absorbent
US6210597B1 (en) 1997-09-25 2001-04-03 Tdk Corporation Radio wave absorbent
US7238298B2 (en) * 2003-10-06 2007-07-03 Tdk Corporation Ni-Cu-Zn-based ferrite material and process for the production thereof
KR101016501B1 (en) * 2007-12-11 2011-02-24 루유안 동양구앙 마그네틱 머티리얼 컴퍼니 리미티드 A NiCuZn ferrite and its manufacturing methods thereof
RU2592867C1 (en) * 2015-07-27 2016-07-27 Федеральное государственное бюджетное учреждение науки институт физики им. Л.В. Киренского Сибирского отделения Российской академии наук Magnetodielectric oxide ceramic material

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6210597B1 (en) 1997-09-25 2001-04-03 Tdk Corporation Radio wave absorbent
EP1006610A2 (en) * 1998-12-04 2000-06-07 TDK Corporation Radio wave absorbent
US6146545A (en) * 1998-12-04 2000-11-14 Tdk Corporation Radio wave absorbent
EP1006610A3 (en) * 1998-12-04 2001-05-23 TDK Corporation Radio wave absorbent
US7238298B2 (en) * 2003-10-06 2007-07-03 Tdk Corporation Ni-Cu-Zn-based ferrite material and process for the production thereof
KR101016501B1 (en) * 2007-12-11 2011-02-24 루유안 동양구앙 마그네틱 머티리얼 컴퍼니 리미티드 A NiCuZn ferrite and its manufacturing methods thereof
RU2592867C1 (en) * 2015-07-27 2016-07-27 Федеральное государственное бюджетное учреждение науки институт физики им. Л.В. Киренского Сибирского отделения Российской академии наук Magnetodielectric oxide ceramic material

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